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PFIZERPEN® Principal Display Panel (penicillin G potassium)

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Label

NDC 0049-0520-84
Rx only

Buffered
Pfizerpen®
(penicillin G potassium, USP)
For Injection

5,000,000 Units* per vial
(Five million units* per vial)

Intramuscular or Intravenous Use

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Label

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Carton

10 Vials
Buffered

NDC 0049-0520-83
Contains 10 of NDC 0049-0520-84
Rx only

Pfizerpen®
(penicillin G potassium, USP)
For Injection

5,000,000 Units* per vial
(Five million units* per vial)

Intramuscular or Intravenous Use

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 5,000,000 Unit Vial Carton

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Label

NDC 0049-0530-28
Rx only

Buffered
Pfizerpen®
(penicillin G potassium, USP)

20,000,000 Units* per vial

(Twenty million units* per vial)
For Intravenous Infusion Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Label

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Carton

NDC 0049-0530-28
Rx only

1 Vial
Buffered

Pfizerpen®
(penicillin G potassium, USP)

20,000,000
Units*
per vial
(Twenty million units* per vial)

For Intravenous Infusion Only

Pfizer Injectables

PRINCIPAL DISPLAY PANEL - 20,000,000 Unit Vial Carton
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Report Adverse Event
Pfizer Safety

To report an adverse event related to a Pfizer product and you are not part of a clinical trial* for this product, click the link below to submit your information: Pfizer Safety Reporting Site

*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

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FDA Medwatch
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatchor by calling
(800)-332-1088.